Canonical Allele Identifier: PA915977237
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14266
ClinVar RCV Id: RCV000015336 RCV000084517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Leu601Val
CA225417
NM_001123066.4:c.1801C>G